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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548426Generated: October 30, 2026

3-Chloroaniline → 4-[(3-Chlorophenyl)amino]-6-nitro-3-quinolinecarbonitrile

https://huagongshe.com/reaction/548426

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloroanilineHCID 7932—
Reactant4-Chloro-6-nitroquinoline-3-carbonitrileHCID 11085690—
SolventEthanolHCID 702—
Product4-[(3-Chlorophenyl)amino]-6-nitro-3-quinolinecarbonitrileHCID 22466674—

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 10.0 g (42.9 mmol)) 4-chloro-6-nitro-quinoline-3-carbonitrile, 260 ml ethanol, and 5.40 ml 3-chloroaniline was heated to reflux under N2. Removed heat at 4 hours, cooled to 25° C. and added saturated sodium bicarbonate until the pH was basic. Stripped solvents and azeotroped with ethanol. Slurried residue with hexane, collected solid, and air dried. Washed solids with water and dried in vacuo. Dissolved in boiling ethyl acetate, stirred with Darco, and filtered. Stripped solvent and dried residue in vacuo, giving 6.5 g of yellow solid: mass spectrum (electrospray m/e): M+H=325.0, 327.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE042376E1
Source datasetuspto-grants-2011_05
ORD IDord-53dede82bb9e4c36a3147737ad99a09c
Source noteuspto-grants-2011_05